Primary Device ID | 00816849016481 |
NIH Device Record Key | 824c7372-425d-4881-8ddc-3bd0aaa63f02 |
Commercial Distribution Discontinuation | 2024-04-26 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | EndoArmor™ Plus |
Version Model Number | SGE-389-10 |
Catalog Number | SGE-389-10 |
Company DUNS | 021717889 |
Company Name | BOSTON SCIENTIFIC CORPORATION |
Device Count | 10 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00816849016481 [Package] Contains: 08714729989349 Package: [10 Units] Discontinued: 2024-04-26 Not in Commercial Distribution |
GS1 | 08714729989349 [Primary] |
GS1 | 08714729989608 [Unit of Use] |
OEA | Non-surgical isolation gown |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2024-05-17 |
Device Publish Date | 2019-02-18 |
00191506004026 | EndoArmor Gown, Plus |
00816849016481 | EndoArmor Gown, Plus |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() ENDOARMOR 85045904 4060919 Live/Registered |
Endochoice, Inc. 2010-05-23 |